HYALO GYN Vaginal Moisturizing Suppositories Sample - HyaloGYN Vaginal Moisturizing Suppositories are - FIDIA FARMACEUTICI SPA

Duns Number:428453013

Device Description: HyaloGYN Vaginal Moisturizing Suppositories are personal lubricants, for vaginal applicati HyaloGYN Vaginal Moisturizing Suppositories are personal lubricants, for vaginal application, intended to moisturize and lubricate, to enhance the ease and comfort of intimate sexual activity and supplement the body’s natural lubrication. This product is not compatible with natural rubber latex, polyurethane, and polyisoprene condoms. The suppositories are made without parabens. The sample box contains 3 suppositories

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More Product Details

Catalog Number

10000405

Brand Name

HYALO GYN Vaginal Moisturizing Suppositories Sample

Version/Model Number

10000405

Device Commercial Distribution Status

In Commercial Distribution

Commercial Distribution End Date

-

Issuing Agency

In HIBCC

Product Characteristics

MRI safety Status

Labeling does not contain MRI Safety Information

Device required to be labeled as containing natural rubber latex or dry natural rubber (21 CFR 801.437)

-

Device labeled as "Not made with natural rubber latex"

-

For Single-Use

-

Prescription Use (Rx)

-

Over the Counter (OTC)

Yes

Kit

-

Combination Product

-

Human Cell, Tissue or Cellular or Tissue-Based Product (HCT/P)

-

FDA Premarket Submission

K191052

Product Code Details

Product Code

NUC

Product Code Name

Lubricant, Personal

Device Record Status

Public Device Record Key

0f6109b6-81cc-450f-99ab-bbe2f7b93604

Public Version Date

April 02, 2021

Public Version Number

1

DI Record Publish Date

March 25, 2021

Additional Identifiers

Package DI Number

None

Quantity per Package

-

Contains DI Package

-

Package Discontinue Date

-

Package Status

-

Package Type

-

"FIDIA FARMACEUTICI SPA" Characteristics
Device Class Device Class Description No of Devices
2 A medical device with a moderate to high risk that requires special controls. 8
3 A medical device with high risk that requires premarket approval 5